D. Ergeç

发表

The Frequency and the Effects of 21‐Hydroxylase Gene Defects in Congenital Adrenal Hyperplasia Patients

F. Eren, T. Akçay, A. Bereket, 2014, Annals of human genetics.

Investigation of the association between mitochondrial DNA and p53 gene mutations in transitional cell carcinoma of the bladder.

L. Turkeri, K. Ulucan, D. Kıraç, 2016, Oncology letters.

Investigation of the association between mitochondrial DNA and p 53 gene mutations in transitional cell carcinoma of the bladder

L. Turkeri, K. Ulucan, D. Kıraç, 2022 .

Detection of Y chromosome microdeletions and mitochondrial DNA mutations in male infertility patients.

T. Tarcan, K. Ulucan, D. Kıraç, 2012, Genetics and molecular research : GMR.

Molecular and cytogenetic evaluation of Y chromosome in spontaneous abortion cases

T. Tarcan, K. Ulucan, D. Kıraç, 2010 .

Effects of ACE polymorphisms and other risk factors on the severity of coronary artery disease.

M. Agirbasli, K. Ulucan, D. Kıraç, 2013, Genetics and molecular research : GMR.

Detection of mitochondrial DNA mutations in nonmuscle invasive bladder cancer.

L. Turkeri, K. Ulucan, D. Kıraç, 2012, Genetic testing and molecular biomarkers.

Regional dispersion of non-syndromic cleft lip with/without palate Turkish children patients and possible geographical effects

T. Akçay, Burak Ersoy, K. Ulucan, 2012 .

The effect of polymorphic metabolism enzymes on serum phenytoin level

M. Uzan, F. Onat, C. Ozkara, 2015, Neurological Sciences.

Coding Regions of MSX1 Do Not Contribute to Non-Syndromic Cleft Lip With/Without Palate in Turkish Patients

M. Konuk, T. Akçay, B. Aksoy, 2014 .